Device
Wide Footprint w/ Cutout Reusable Guide
Manufacturer
ARTHREX, INC.
Model: AR-3650WF Catalog: AR-3650WF DI: 00888867549760 Status: New MRI: Labeling does not contain MRI Safety Information Single-use: No Rx: Yes OTC: No
First Published: 2026-05-05 Current Version: 2026-05-13
Description
Wide Footprint w/ Cutout Reusable Guide
Sterilization
Method Types - Sterilization Method: Moist Heat or Steam Sterilization
Device Sterile: No
Sterilization Prior To Use: Yes
Regulatory & Distribution
Record Status: Published
Version Number: 1
Record Key: d4e6a806-b097-45bf-b8ec-b080a3cdd698
Distribution Status: In Commercial Distribution
DUNS Number: 131747628
Device Count: 1
DM Exempt: No
Premarket Exempt: Yes
HCT/P: No
Kit: No
Combination Product: No
Lot/Batch Tracked: Yes
Serial Number Tracked: No
Manufacturing Date Tracked: Yes
Expiration Date Tracked: No
Donation ID Number Tracked: No
Labeled Contains NRL: No
Labeled No NRL: No
Identifiers
Device ID: 00888867549760
Type: Primary
Issuing Agency: GS1
GMDN
Code: 35095
Name: Surgical drill guide, reusable
Definition:
A manual surgical device designed to simultaneously place, angle, and guide a rotating surgical drill on hard tissue (e.g., bone); some types are also intended for guiding bone-coring instruments (e.g., keel punch). It is designed in a tubular form or with guiding holes and may have serrations at its distal end to enable firm placement on hard tissue surfaces (it is not bored into the tissue); it can have a handle or be held by another device (e.g., orthopaedic jig), and typically allows protection of the surrounding soft tissue during surgery. It is typically made of metal and may have graduations along its length; it is not custom-made for a specific patient. This is a reusable device.
FDA Product Codes
LXH
Orthopedic manual surgical instrument